Label: AQUAPHOR LIP REPAIR STICK AND SUNSCREEN- avobenzone, homosalate, octisalate, octocrylene, stick
- NDC Code(s): 10356-130-25, 10356-130-41
- Packager: Beiersdorf Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 28, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- STOP USE
- KEEP OUT OF REACH OF CHILDREN
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DOSAGE & ADMINISTRATION
For sunscreen use
- apply liberally at least 15 minutes before sun exposure
- use a water resistant sunscreen if swimming or sweating
- reapply at least every two hours
- Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk regularly use a sunscreen with a Broad SpectrumSPFvalue of 15 or higher and other sun protection measures including: •limit time in the sun, especially from 10 a.m. – 2 p.m. •wear long-sleeved shirts, pants, hats, and sunglasses
- children under 6 months of age: Ask a doctor
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INACTIVE INGREDIENT
Inactive ingredients
Octyldodecanol, Ricinus Communis (Castor) Seed Oil, Beeswax, Bis-Diglyceryl Polyacyladipate-2, Butyrospermum Parkii (Shea) Butter, Hydrogenated Castor OIl, Helianthus Annuus (Sunflower) Seed Wax, Cetearyl Alcohol, Dimethicone, Simmondsia Chinensis (Jojoba) Seed Oil, Copernicia Cerifera (Carnauba) Wax, Tocopheryl Acetate, Ascorbyl Palmitate, Tocopherol. - QUESTIONS
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
AQUAPHOR LIP REPAIR STICK AND SUNSCREEN
avobenzone, homosalate, octisalate, octocrylene, stickProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:10356-130 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE 9 g in 100 g OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE 4.5 g in 100 g AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE 3 g in 100 g OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE 9 g in 100 g Inactive Ingredients Ingredient Name Strength HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV) CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S) HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY) CARNAUBA WAX (UNII: R12CBM0EIZ) ASCORBYL PALMITATE (UNII: QN83US2B0N) SHEA BUTTER (UNII: K49155WL9Y) BIS-DIGLYCERYL POLYACYLADIPATE-2 (UNII: 6L246LAM9T) .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) TOCOPHEROL (UNII: R0ZB2556P8) DIMETHICONE (UNII: 92RU3N3Y1O) OCTYLDODECANOL (UNII: 461N1O614Y) CASTOR OIL (UNII: D5340Y2I9G) YELLOW WAX (UNII: 2ZA36H0S2V) JOJOBA OIL (UNII: 724GKU717M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:10356-130-25 4.8 g in 1 TUBE; Type 0: Not a Combination Product 11/15/2021 2 NDC:10356-130-41 2 in 1 BLISTER PACK 11/15/2021 2 NDC:10356-130-25 4.8 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 11/15/2021 Labeler - Beiersdorf Inc (001177906)
